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Results: 1 to 20 of 432

1.

Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors.

Ciesielski TH, Pendergrass SA, White MJ, Kodaman N, Sobota RS, Huang M, Bartlett J, Li J, Pan Q, Gui J, Selleck SB, Amos CI, Ritchie MD, Moore JH, Williams SM.

BioData Min. 2014 Jun 30;7:10. doi: 10.1186/1756-0381-7-10. eCollection 2014.

PMID:
25071867
[PubMed]
2.

Genetic Variants in CYP2R1, CYP24A1 and VDR Modify the Efficacy of Vitamin D3 Supplementation for Increasing Serum 25-Hydroxyvitamin D Levels in a Randomized Controlled Trial.

Barry EL, Rees JR, Peacock JL, Mott LA, Amos CI, Bostick RM, Figueiredo JC, Ahnen DJ, Bresalier RS, Burke CA, Baron JA.

J Clin Endocrinol Metab. 2014 Jul 29:jc20141389. [Epub ahead of print]

PMID:
25070320
[PubMed - as supplied by publisher]
3.

Identification of a melanoma susceptibility locus and somatic mutation in TET2.

Song F, Amos CI, Lee JE, Lian CG, Fang S, Liu H, MacGregor S, Iles MM, Lindeman NI, Montgomery GW, Duffy DL, Cust AE, Jenkins MA, Whiteman DC, Kefford RF, Giles GG, Armstrong BK, Aitken JF, Hopper JL, Brown KM, Martin NG, Mann GJ, Bishop DT, Newton Bishop JA; the GenoMEL consortium, Kraft P, Qureshi AA, Kanetsky PA, Hayward NK, Hunter DJ, Wei Q, Han J.

Carcinogenesis. 2014 Jun 30. pii: bgu140. [Epub ahead of print]

PMID:
24980573
[PubMed - as supplied by publisher]
4.

Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.

Wang Y, McKay JD, Rafnar T, Wang Z, Timofeeva MN, Broderick P, Zong X, Laplana M, Wei Y, Han Y, Lloyd A, Delahaye-Sourdeix M, Chubb D, Gaborieau V, Wheeler W, Chatterjee N, Thorleifsson G, Sulem P, Liu G, Kaaks R, Henrion M, Kinnersley B, Vallée M, LeCalvez-Kelm F, Stevens VL, Gapstur SM, Chen WV, Zaridze D, Szeszenia-Dabrowska N, Lissowska J, Rudnai P, Fabianova E, Mates D, Bencko V, Foretova L, Janout V, Krokan HE, Gabrielsen ME, Skorpen F, Vatten L, Njølstad I, Chen C, Goodman G, Benhamou S, Vooder T, Välk K, Nelis M, Metspalu A, Lener M, Lubiński J, Johansson M, Vineis P, Agudo A, Clavel-Chapelon F, Bueno-de-Mesquita HB, Trichopoulos D, Khaw KT, Johansson M, Weiderpass E, Tjønneland A, Riboli E, Lathrop M, Scelo G, Albanes D, Caporaso NE, Ye Y, Gu J, Wu X, Spitz MR, Dienemann H, Rosenberger A, Su L, Matakidou A, Eisen T, Stefansson K, Risch A, Chanock SJ, Christiani DC, Hung RJ, Brennan P, Landi MT, Houlston RS, Amos CI.

Nat Genet. 2014 Jul;46(7):736-41. doi: 10.1038/ng.3002. Epub 2014 Jun 1.

PMID:
24880342
[PubMed - in process]
5.

Molecular profiling of appendiceal epithelial tumors using massively parallel sequencing to identify somatic mutations.

Liu X, Mody K, de Abreu FB, Pipas JM, Peterson JD, Gallagher TL, Suriawinata AA, Ripple GH, Hourdequin KC, Smith KD, Barth RJ Jr, Colacchio TA, Tsapakos MJ, Zaki BI, Gardner TB, Gordon SR, Amos CI, Wells WA, Tsongalis GJ.

Clin Chem. 2014 Jul;60(7):1004-11. doi: 10.1373/clinchem.2014.225565. Epub 2014 May 12.

PMID:
24821835
[PubMed - in process]
6.

Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortia.

Park SL, Fesinmeyer MD, Timofeeva M, Caberto CP, Kocarnik JM, Han Y, Love SA, Young A, Dumitrescu L, Lin Y, Goodloe R, Wilkens LR, Hindorff L, Fowke JH, Carty C, Buyske S, Schumacher FR, Butler A, Dilks H, Deelman E, Cote ML, Chen W, Pande M, Christiani DC, Field JK, Bickebller H, Risch A, Heinrich J, Brennan P, Wang Y, Eisen T, Houlston RS, Thun M, Albanes D, Caporaso N, Peters U, North KE, Heiss G, Crawford DC, Bush WS, Haiman CA, Landi MT, Hung RJ, Kooperberg C, Amos CI, Le Marchand L, Cheng I.

J Natl Cancer Inst. 2014 Apr;106(4):dju061. doi: 10.1093/jnci/dju061. Epub 2014 Mar 28.

PMID:
24681604
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Underestimation of risk of a BRCA1 or BRCA2 mutation in women with high-grade serous ovarian cancer by BRCAPRO: a multi-institution study.

Daniels MS, Babb SA, King RH, Urbauer DL, Batte BA, Brandt AC, Amos CI, Buchanan AH, Mutch DG, Lu KH.

J Clin Oncol. 2014 Apr 20;32(12):1249-55. doi: 10.1200/JCO.2013.50.6055. Epub 2014 Mar 17.

PMID:
24638001
[PubMed - indexed for MEDLINE]
8.

Genome-wide association tests of inversions with application to psoriasis.

Ma J, Xiong M, You M, Lozano G, Amos CI.

Hum Genet. 2014 Aug;133(8):967-74. doi: 10.1007/s00439-014-1437-1. Epub 2014 Mar 13.

PMID:
24623382
[PubMed - in process]
9.

A network-based kernel machine test for the identification of risk pathways in genome-wide association studies.

Freytag S, Manitz J, Schlather M, Kneib T, Amos CI, Risch A, Chang-Claude J, Heinrich J, Bickeböller H.

Hum Hered. 2013;76(2):64-75. doi: 10.1159/000357567. Epub 2014 Jan 14.

PMID:
24434848
[PubMed - in process]
10.

Axonal guidance signaling pathway interacting with smoking in modifying the risk of pancreatic cancer: a gene- and pathway-based interaction analysis of GWAS data.

Tang H, Wei P, Duell EJ, Risch HA, Olson SH, Bueno-de-Mesquita HB, Gallinger S, Holly EA, Petersen G, Bracci PM, McWilliams RR, Jenab M, Riboli E, Tjønneland A, Boutron-Ruault MC, Kaaks R, Trichopoulos D, Panico S, Sund M, Peeters PH, Khaw KT, Amos CI, Li D.

Carcinogenesis. 2014 May;35(5):1039-45. doi: 10.1093/carcin/bgu010. Epub 2014 Jan 13.

PMID:
24419231
[PubMed - indexed for MEDLINE]
11.

Serrated and adenomatous polyp detection increases with longer withdrawal time: results from the New Hampshire Colonoscopy Registry.

Butterly L, Robinson CM, Anderson JC, Weiss JE, Goodrich M, Onega TL, Amos CI, Beach ML.

Am J Gastroenterol. 2014 Mar;109(3):417-26. doi: 10.1038/ajg.2013.442. Epub 2014 Jan 7.

PMID:
24394752
[PubMed - indexed for MEDLINE]
12.

Joint effect of multiple common SNPs predicts melanoma susceptibility.

Fang S, Han J, Zhang M, Wang LE, Wei Q, Amos CI, Lee JE.

PLoS One. 2013 Dec 31;8(12):e85642. doi: 10.1371/journal.pone.0085642. eCollection 2013.

PMID:
24392023
[PubMed - in process]
Free PMC Article
13.

Routine use of the Ion Torrent AmpliSeq™ Cancer Hotspot Panel for identification of clinically actionable somatic mutations.

Tsongalis GJ, Peterson JD, de Abreu FB, Tunkey CD, Gallagher TL, Strausbaugh LD, Wells WA, Amos CI.

Clin Chem Lab Med. 2014 May;52(5):707-14. doi: 10.1515/cclm-2013-0883.

PMID:
24334431
[PubMed - in process]
14.

The national alopecia areata registry-update.

Duvic M, Christiano AM, Hordinsky MK, Norris DA, Price VH, Amos CI.

J Investig Dermatol Symp Proc. 2013 Dec;16(1):S53. doi: 10.1038/jidsymp.2013.20. No abstract available.

PMID:
24326558
[PubMed - in process]
Free Article
15.

Health-Related Quality of Life (HRQoL) in alopecia areata patients-a secondary analysis of the National Alopecia Areata Registry Data.

Shi Q, Duvic M, Osei JS, Hordinsky MK, Norris DA, Price VH, Amos CI, Christiano AM, Mendoza TR.

J Investig Dermatol Symp Proc. 2013 Dec;16(1):S49-50. doi: 10.1038/jidsymp.2013.18.

PMID:
24326555
[PubMed - in process]
Free Article
16.

Findings from the Peutz-Jeghers syndrome registry of uruguay.

Tchekmedyian A, Amos CI, Bale SJ, Zhu D, Arold S, Berrueta J, Nabon N, McGarrity T.

PLoS One. 2013 Nov 19;8(11):e79639. doi: 10.1371/journal.pone.0079639. eCollection 2013.

PMID:
24260271
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Natural and orthogonal model for estimating gene-gene interactions applied to cutaneous melanoma.

Xiao F, Ma J, Cai G, Fang S, Lee JE, Wei Q, Amos CI.

Hum Genet. 2014 May;133(5):559-74. doi: 10.1007/s00439-013-1392-2. Epub 2013 Nov 17.

PMID:
24241239
[PubMed - indexed for MEDLINE]
18.

Genes-environment interactions in obesity- and diabetes-associated pancreatic cancer: a GWAS data analysis.

Tang H, Wei P, Duell EJ, Risch HA, Olson SH, Bueno-de-Mesquita HB, Gallinger S, Holly EA, Petersen GM, Bracci PM, McWilliams RR, Jenab M, Riboli E, Tjønneland A, Boutron-Ruault MC, Kaaks R, Trichopoulos D, Panico S, Sund M, Peeters PH, Khaw KT, Amos CI, Li D.

Cancer Epidemiol Biomarkers Prev. 2014 Jan;23(1):98-106. doi: 10.1158/1055-9965.EPI-13-0437-T. Epub 2013 Oct 17.

PMID:
24136929
[PubMed - in process]
19.

A unified framework integrating parent-of-origin effects for association study.

Xiao F, Ma J, Amos CI.

PLoS One. 2013 Aug 26;8(8):e72208. doi: 10.1371/journal.pone.0072208. eCollection 2013.

PMID:
23991061
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Genome-wide association study of dermatomyositis reveals genetic overlap with other autoimmune disorders.

Miller FW, Cooper RG, Vencovský J, Rider LG, Danko K, Wedderburn LR, Lundberg IE, Pachman LM, Reed AM, Ytterberg SR, Padyukov L, Selva-O'Callaghan A, Radstake TR, Isenberg DA, Chinoy H, Ollier WE, O'Hanlon TP, Peng B, Lee A, Lamb JA, Chen W, Amos CI, Gregersen PK; Myositis Genetics Consortium.

Arthritis Rheum. 2013 Dec;65(12):3239-47. doi: 10.1002/art.38137.

PMID:
23983088
[PubMed - indexed for MEDLINE]

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